Allele Registry

Canonical Allele Identifier: PA102736

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056823

RCV000192161

ClinVar Variation:

66430

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Leu359Pro	CA217104 NM_002055.5:c.1076T>C